North Woods Derma Gel Clear

Product NDC
53125-801
11-digit product format
531250801
Labeler code
53125
Product ID
53125-801_40a72db6-d505-3e66-e063-6294a90a6566
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
Superior Chemical Corporation
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-08-01
Substance
ALCOHOL
Active strength
.7 mL/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage53125-80153125-801-09DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
North Woods Derma Gel Clear
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL.7 mL/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
581662Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
abbd099a-8d89-80a0-e053-2a95a90a24fcAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53125-801-04North Woods Derma Gel Clear3780 mL in 1 BOTTLE, PLASTICGEL37804
53125-801-09North Woods Derma Gel Clear500 mL in 1 BOTTLE, PUMPGEL5004
53125-801-29North Woods Derma Gel Clear1000 mL in 1 BAGGEL10004
53125-801-57North Woods Derma Gel Clear550 mL in 1 BOTTLE, PUMPGEL5504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53125-801NORTH WOODS DERMA GEL CLEAR (ALCOHOL) GEL [SUPERIOR CHEMICAL CORPORATION]3Current NDC, Legacy NDC, 4 package rows20241120_abbd099a-8d89-80a0-e053-2a95a90a24fc.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
North Woods Derma Gel ClearALCOHOLSuperior Chemical Corporationabbd099a-8d89-80a0-e053-2a95a90a24fc2025-10-08WarningsExact identifier
ndc (product): 53125-801

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSNabbd099a-8d89-80a0-e053-2a95a90a24fc4
581662ethanol 0.7 ML/ML Topical GelSCDabbd099a-8d89-80a0-e053-2a95a90a24fc4
581662ethanol 70 % Topical GelSYabbd099a-8d89-80a0-e053-2a95a90a24fc4
581662ethyl alcohol 70 % Topical GelSYabbd099a-8d89-80a0-e053-2a95a90a24fc4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53125-801-04531250801043780 mL in 1 BOTTLE, PLASTIC (53125-801-04) 3780 ml2019-08-010000-00-00NoNoCurrent
53125-801-0953125080109500 mL in 1 BOTTLE, PUMP500 mlHistorical
53125-801-29531250801291000 mL in 1 BAG (53125-801-29) 1000 ml2019-08-01NoNoCurrent
53125-801-5753125080157550 mL in 1 BOTTLE, PUMP (53125-801-57) 550 ml2019-08-010000-00-00NoNoCurrent
53125-801-8853125080188500 mL in 1 BOTTLE, PUMP (53125-801-88) 500 ml2019-08-010000-00-00NoNoCurrent